Koyasu Sho, Kobayashi Minoru, Goto Yoko, Hiraoka Masahiro, Harada Hiroshi
Laboratory of Cancer Cell Biology, Department of Genome Dynamics, Radiation Biology Center, Kyoto University, Kyoto, Japan.
Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
Cancer Sci. 2018 Mar;109(3):560-571. doi: 10.1111/cas.13483. Epub 2018 Jan 27.
Hypoxia-inducible factor 1 (HIF-1) is a transcriptional activator of various genes related to cellular adaptive responses to hypoxia. Dysfunctions in the regulatory systems of HIF-1 activity have been implicated in the pathogenesis of various diseases including malignant tumors and, thus, elucidating the molecular mechanisms underlying the activation of HIF-1 is eagerly desired for the development of novel anti-cancer strategies. The importance of oxygen-dependent and ubiquitin-mediated proteolysis of the regulatory subunit of HIF-1 (HIF-1α) was first reported in 1997. Since then, accumulating evidence has shown that HIF-1α may become stable and active even under normoxic conditions; for example, when disease-associated genetic and functional alterations in some genes trigger the aberrant activation of HIF-1 regardless of oxygen conditions. We herein review the last two decades of knowledge, since 1997, on the regulatory mechanisms of HIF-1 activity from conventional oxygen- and proteolysis-dependent mechanisms to up-to-the-minute information on cancer-associated genetic and functional alteration-mediated mechanisms.
缺氧诱导因子1(HIF-1)是一种转录激活因子,可激活多种与细胞缺氧适应性反应相关的基因。HIF-1活性调节系统的功能障碍与包括恶性肿瘤在内的多种疾病的发病机制有关,因此,阐明HIF-1激活的分子机制对于开发新型抗癌策略具有迫切需求。1997年首次报道了HIF-1调节亚基(HIF-1α)的氧依赖性和泛素介导的蛋白水解的重要性。从那时起,越来越多的证据表明,即使在常氧条件下,HIF-1α也可能变得稳定并具有活性;例如,当某些基因中与疾病相关的遗传和功能改变触发HIF-1的异常激活而不受氧条件影响时。本文回顾了自1997年以来的二十年知识,内容涵盖了从传统的氧依赖性和蛋白水解依赖性机制到最新的癌症相关遗传和功能改变介导机制的HIF-1活性调节机制。